The purpose of this study was to examine the effect of ultrahigh molecular
weight polyethylene resin type and manufacturing method on wear of Miller-G
alante I and II tibial knee components. Thirteen Miller-Galante I and 10 Mi
ller-Galante II components were retrieved at revision surgery. The Miller-G
alante I tibial components were made by direct compression molding of Hi-fa
x 1900 resin and the Miller-Galante II tibial components were made by machi
ning from ram extruded rod of GUR 415 resin. Both generations were gamma ra
diation sterilized in air. The Miller-Galante I retrievals had significantl
y more wear damage in the form of scratching and embedded metallic debris,
whereas the Miller-Galante II retrievals had significantly more wear damage
in the form of delamination. For the implants with an implantation time of
5 years or more, the Miller-Galante II polyethylene had a significantly gr
eater maximum density value than did the Miller-Galante I polyethylene. Exa
mination of thin sections of the Miller-Galante II components revealed that
delamination occurred through a subsurface region of severely oxidatively
degraded polyethylene; no such sub-surface degraded region was observed for
the Miller-Galante I components. The results of this study suggest that de
lamination of polyethylene tibial components that have been gamma radiation
sterilized (in air) is influenced by resin type or manufacturing method or
both.